The polypill: An effective approach to increasing adherence and reducing cardiovascular event risk

Eur J Prev Cardiol. 2017 Feb;24(3):297-310. doi: 10.1177/2047487316674817. Epub 2016 Oct 22.

Abstract

Background Despite a wide range of medications being available for the prevention of cardiovascular events such as stroke, myocardial infarction and mortality in both a primary and secondary setting, patient adherence to complex therapy regimens involving different drug classes remains low worldwide. Combining antiplatelet, antihypertensive, lipid-lowering and potentially further drugs into one 'polypill' has the potential to increase adherence, thereby reducing risk factors to a greater extent and for a longer duration. The World Health Organization has recently highlighted increased adherence as a key development need for reducing cardiovascular disease. Methods Recent clinical trial data regarding adherence, reductions in cardiovascular risk and outcomes, safety and tolerability and the cost-effectiveness of the polypill approach are summarised and reviewed. In addition, ongoing trials and the questions they intend to answer are considered. References were retrieved from a PubMed literature search (date range 1990-2016) using the terms 'polypill', 'cardiovascular events' and 'adherence', and selected based on relevance. The website www.clinicaltrials.gov was also consulted for the identification of ongoing trials. Conclusions To date, the polypill approach has been conclusively shown to increase adherence relative to usual care in all patients, with those in a primary care setting or with poor baseline adherence potentially standing to benefit most. Concomitant risk factor reductions have also been suggested. However, whether this translates into a reduction in cardiovascular events and generates good cost-effectiveness in a given healthcare environment is currently under further investigation.

Keywords: Adherence; LDL-cholesterol; cardiovascular events/outcomes; polypill; systolic blood pressure.

Publication types

  • Review

MeSH terms

  • Administration, Oral
  • Antihypertensive Agents / administration & dosage
  • Cardiovascular Agents / administration & dosage*
  • Cardiovascular Agents / adverse effects
  • Cardiovascular Agents / economics
  • Cardiovascular Diseases / diagnosis
  • Cardiovascular Diseases / economics
  • Cardiovascular Diseases / epidemiology
  • Cardiovascular Diseases / prevention & control*
  • Cost Savings
  • Cost-Benefit Analysis
  • Drug Combinations
  • Drug Costs
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / administration & dosage
  • Medication Adherence*
  • Platelet Aggregation Inhibitors / administration & dosage
  • Preventive Health Services / economics
  • Preventive Health Services / methods*
  • Protective Factors
  • Risk Assessment
  • Risk Factors
  • Tablets

Substances

  • Antihypertensive Agents
  • Cardiovascular Agents
  • Drug Combinations
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Platelet Aggregation Inhibitors
  • Tablets